Tag | Content |
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EnhancerAtlas ID | HS050-45508 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr22:46980090-46981020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLIS2 | MA0736.1 | chr22:46980499-46980513 | GACCCCCCGGGAAG | + | 6.07 | GLIS3 | MA0737.1 | chr22:46980499-46980513 | GACCCCCCGGGAAG | + | 6.05 | ZNF263 | MA0528.1 | chr22:46980622-46980643 | GAGGGAAGAAGGGAGGGAGGC | + | 6.06 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23135 | chr22:46979324-46980510 | Colon_Crypt_1 | SE_23756 | chr22:46980171-46980723 | Colon_Crypt_2 | SE_24734 | chr22:46979356-46980900 | Colon_Crypt_3 | SE_26636 | chr22:46979812-46981163 | Esophagus | SE_31503 | chr22:46979960-46980955 | Gastric | SE_40615 | chr22:46979218-46981201 | Left_Ventricle | SE_49480 | chr22:46980263-46981085 | Right_Ventricle | SE_59021 | chr22:46957262-46990616 | Ly3 | SE_61894 | chr22:46957289-46995869 | Toledo | SE_65649 | chr22:46979892-46983822 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I046584 | chr22 | 46980581 | 46980730 |
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Enhancer Sequence | CAGGCCTAGA GTCAGCCCCT TCTGCAGGGA GCCCGGGTTC CTTTTGTTGG AGGGCAGAAT 60 CGGAAACCAA GATCCAGGTG GCGGGTACGC TCATCACTAC CGGGGTGTCA TTGCTTCTGG 120 GCCCTCTTAG CTGACAGCAA GGAAATGCAC GTGTGAGCTG ACGCGCACAT ATGTACGTGT 180 CTCTGCCTGT GTCCGCGTGT AGCCTCCTGT ACCTGTATTG AGCAAAGTGT GAGTTCGCGC 240 CGCTGATGAA CTCTGATCCG TTTCCTGCAT GGATCTTTCT CGTCTCCTTT CTTGCAGATC 300 AATTCGTGTC TATTCAAGCA GCAGGAAGCC AGACTCCCAC CGCTTGCCAC ACATCTACTT 360 AATTGTTAGT ACCGGTGTGT CTGCGTAGTG GGACTGGAGT TGTTAGTGGG ACCCCCCGGG 420 AAGCAGTTCC CGATCCCTTG GCTTCGAGCC CGGGCTCCCG GTATGCTGCC GCAGCATGGC 480 TGGCTGGGGC TGGGGAGGGG CCGCCACCTC CCCAACATGA TTCCACGACT TAGAGGGAAG 540 AAGGGAGGGA GGCTGCAGGA GAACCAGGGA CTTCCCTGCT GTGCTTAGTC AGCCCGGCCC 600 CGCAGGGACG GGCACGGGCT TGGCGTTGCT TTGAGACGTG AAAGTGGGGC TGACTTAGAA 660 CGCATCCCAG AGTCCGGCCT CCTCGGGGAA GGAGGAGAAA GGCTGCCGGC GGGACGCTTT 720 AGAGCTCAGA CAAATCTCCG ACTCCATCCT GGCCAGGTCT GTCCCCTCTC TGCCTCTGAA 780 CTTGCCACCC TGGCAGGGGA CGGCCTTTGA AAAGATCTAC AGAGCCGCAT CTGCTGGGCT 840 TTCTGTTAAG CATCTTTCAT TCAGGAATGC GTCAGGCCCT TGCAGAAGTT TTGGGAAGAG 900 AGAGAACCAG GTGGTCACTC CTCGTCTGCT 930
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